A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033552



Internal ID18776085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19104664..19131868hg38UCSC Ensembl
Innerchr9:19104662..19131866hg19UCSC Ensembl
Innerchr9:19094662..19121866hg18UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3827205
hg1927205
hg1827205
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690677
Samples
Known GenesPLIN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033552
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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